A simplified six item checklist for screening for fragile X syndrome in the pediatric population von Giangreco, Cheryl A., Steele, Mark W., Aston, Christopher E., Cummins, James H., Wenger, Sharon L.

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Relaxation of imprinting in Prader-Willi syndrome von ROGAN, P. K, SEIP, J. R, WHITE, L. M, WENGER, S. L, STEELE, M. W, SPERLING, M. A, MENON, R, KNOLL, J. H. M

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X/Y Translocations Resulting from Recombination Between Homologous Sequences on Xp and Yq von Yen, Pauline H., Tsai, Siao-Ping, Wenger, Sharon L., Steele, Mark W., Mohandas, Thuluvancheri K., Shapiro, Larry J.

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On the economics of clinical genetic services in academic institutions von STEELE, M. W

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Chromosomal abnormalities in a psychiatric population von Lewis, Karen E., Lubetsky, Martin J., Wenger, Sharon L., Steele, Mark W.

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A molecular anatomical analysis of mosaic trisomy 16 von GREALLY, J. M, NEISWANGER, K, CUMMINS, J. H, BOONE, L. Y, LENKEY, S. G, WENGER, S. L, LEWIS, J. L, FISCHER, D, PAUL, R. A, STEELE, M. W

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Terminal 2q deletion-a recognizable syndrome von Wenger, Sharon L., Boone, Leslie Y., Surti, Urvashi, Steele, Mark W.

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HSV Esophagitis in an Immunocompetent 17-Year-Old von Rajasekaran, Vedika, Rahaman, Victoria, Hou, Xing, Steele, Russell W.

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Clinical consequences of deletion 1p35 von Wenger, S L, Steele, M W, Becker, D J

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X chromosome imprinting in fragile X syndrome von WEI-DONG YU, WENGER, S. L, STEELE, M. W

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Cardiometabolic Risk in Canada: A Detailed Analysis and Position Paper by the Cardiometabolic Risk Working Group von Leiter, Lawrence A., MD, FRCPC, FACP, Fitchett, David H., MD, FRCPC, Gilbert, Richard E., MD, PhD, FRCPC, FRACP, Gupta, Milan, MD, FRCPC, Mancini, G.B. John, MD, FRCPC, FACC, McFarlane, Philip A., MD, PhD, FRCPC, Ross, Robert, PhD, Teoh, Hwee, PhD, Verma, Subodh, MD, PhD, FRCSC, FAHA, Anand, Sonia, MD, PhD, FRCPC, Camelon, Kathryn, RD, CDE, Chow, Chi-Ming, MDCM, MSc, FRCPC, FACC, Cox, Jafna L., BA, MD, FRCPC, FACC, Després, Jean-Pierre, PhD, FAHA, Genest, Jacques, MD, FRCPC, Harris, Stewart B., MD, MPH, FCFP, FACPM, Lau, David C.W., MD, PhD, FRCPC, Lewanczuk, Richard, MD, PhD, Liu, Peter P., MD, MSc, FRCPC, Lonn, Eva M., MD, MSc, FRCPC, FACC, McPherson, Ruth, MD, PhD, FRCPC, Poirier, Paul, MD, PhD, FRCPC, FACC, FAHA, Qaadri, Shafiq, MD, MPP, Rabasa-Lhoret, Rémi, MD, PhD, Rabkin, Simon W., MD, FRCPC, FACC, Sharma, Arya M., MD, PhD, FRCPC, Steele, Andrew W., MD, FRCPC, Stone, James A., MD, PhD, FRCPC, FAACVPR, FACC, Tardif, Jean-Claude, MD, FRCPC, FACC, Tobe, Sheldon, MD, FRCPC, Ur, Ehud, MB, FRCP

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Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations von Kurnit, D.M., Steele, M.W., Dibbins, A., Pinsky, L.

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CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS von Steele, MarkW, Roy Breg, W.

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Lack of impact of undergraduate genetic courses on the teaching of medical genetics von Steele, M W, Barnhill, B M

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Research squeeze von Steele, Mark W

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Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostoses von DOMINGUEZ, R, YOUNG, L. W, STEELE, M. W, GIRDANY, B. R

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Chromosome mosaicism in hypomelanosis of Ito von Ritter, Catherine L., Steele, Mark W., Wenger, Sharon L., Cohen, Bernard A.

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Prompting Discussions of Youth Violence Using Electronic Previsit Questionnaires in Primary Care: A Cluster Randomized Trial von Riese, Alison, MD, MPH, Mello, Michael J., MD, MPH, Baird, Janette, PhD, Steele, Dale W., MD, MS, Ranney, Megan L., MD, MPH

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Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes von Lin, Angela E., Garver, Kenneth L., Diggans, Gerard, Clemens, Michele, Wenger, Sharon L., Steele, Mark W., Jones, Marilyn C., Israel, Jeannette, Opitz, John M., Reynolds, James F.

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Rash and Fever in a 7-Week-Old Infant von Canares, Therese L., MD, Chang, Brian L., MD, Steele, Dale W., MD, MS

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